Technical Field
[0001] The present invention relates to an adhesive composition and an endoscope device.
Background Art
[0002] It is necessary for an endoscope to make a diameter of a part inserted into a body
cavity (insertion part) as narrow as possible for inserting it into the body cavity,
or the like. Various items are incorporated inside the insertion part to diversify
the functions of the endoscope.
[0003] For example, various tubes are incorporated into the insertion part of the endoscope,
and an adhesive is used for fixing open parts of the tubes to the tip or an operation
part. In addition, an optical system is provided on a hard part of the tip of the
insertion part for observing the inside of a body cavity. The optical system includes
a cover lens and lenses thereof, and a cover lens and lenses thereof for illumination
from a light guide, and an adhesive is used for fixing these lenses on a lens frame
or the hard part of the tip.
[0004] Within the insertion part are further incorporated a light guide for transmitting
light to the tip part, and an image guide for transmitting an image to an eyepiece
part. Fiber bundles, in which a number of fibers are bundled, are used for the light
guide and the image guide. An adhesive is used for fixing the fiber bundles to the
lens frame or the hard part of the tip part.
[0005] As regards an electronic endoscope, in addition to the tubes and fiber bundles described
above, cables, which transmit electric signals to a connector part from a CCD and
the like within the hard part of the tip part, are also incorporated. An adhesive
is used for protecting and fixing the CCD and the like.
[0006] The adhesive is also used for finishing an outer surface of the endoscope. Prior
to the finishing using the adhesive, an edge of a flexible sheath tube is tightly
bound with threads from the outside, which is fixed on a member inside thereof. In
order to secure an insertion property of the flexible sheath tube and prevent loose
threads, an adhesive is coated on the threads. In this way, the finishing of the outer
surface and the fixing of the threads are performed.
[0007] The endoscope is required to be completely sterilized, because it is inserted into
the body cavity of a patient. The endoscope is subjected to a sterilization treatment
using an autoclave with high temperature and high pressure steam, or a sterilization
treatment using a chemical such as peracetic acid or gas (such as hydrogen peroxide
gas or ethylene oxide gas). When a medical device such as an endoscope is subjected
to the sterilization treatment using the autoclave or the chemical, the adhesive layer
can be deteriorated by saturated steam or the chemical, and thus members bonded by
the adhesive may be peeled off from each other.
[0008] JP No. 3806635 proposes that deterioration of an adhesive layer is prevented by incorporating predetermined
filler in the adhesive to enhance a sterilization resistance even after a sterilization
treatment.
JP 2002-238834-A discloses that in order to maintain air tightness and durability of a bonded part
of lenses and a frame in a bonded lens unit even after a sterilization treatment,
the lenses are bonded to the frame using an adhesive containing a thermosetting resin
such as an epoxy resin, and a filler.
JP No. 4875790 discloses that when certain silica is contained as a filler, an adhesive layer which
has sufficient durability against various disinfection methods and which hardly transmits
steam can be obtained.
Summary of Invention
Technical Problem
[0009] Some of the conventional adhesives, however, have insufficient durability when the
sterilization treatment is performed multiple times, and if the sterilization treatment
is repetitively performed, the members bonded through the adhesive layer may sometimes
be peeled off from each other. In addition, the sterilization treatment may change
the color of the adhesive layer, cause cracks in the adhesive layer, or dissolve the
adhesive layer, thus resulting in a deteriorated appearance of the adhesive layer
in the endoscope outer surface.
[0010] When a sterilization treatment using hydrogen peroxide plasma (gas sterilization
treatment) is performed, the adhesive layer can be more severely deteriorated. For
example, the adhesive layer may be peeled off from a forming member, or the surface
of the adhesive layer may change to a foamy state, which reduces the performance.
[0011] The present invention has been made in view of the circumstance described above,
and aims at providing an adhesive composition capable of forming an adhesive layer,
which has excellent sterilization resistance and which can maintain excellent adhesive
strength and appearance, even after a sterilization with hydrogen peroxide plasma.
[0012] The present invention also aims at providing an endoscope device in which an adhesive
layer, which bonds constituent materials to each other or coats the constituent materials,
has an excellent sterilization resistance and can maintain excellent adhesive strength
and appearance after a sterilization with hydrogen peroxide plasma.
Solution to Problem
[0013] A solution to the problems described above is an adhesive composition comprising
a main agent containing at least one epoxy resin selected from a bisphenol A epoxy
resin, a bisphenol F epoxy resin, and a phenol novolac epoxy resin, and an acrylic
rubber; a curing agent containing xylylene diamine, a filler containing silica; and
an ion exchanger.
[0014] The ion exchanger can contain at least one substance selected from styrene, derivatives
thereof, divinyl benzene, derivatives thereof, bismuth, antimony, zirconium, magnesium,
and aluminum.
[0015] The ion exchanger may be contained in a content of 0.8 to 12 parts by mass based
on 100 parts by mass of the main agent.
[0016] The endoscope device, which is one embodiment of the present invention, is characterized
in that at least two constituent members are bonded to each other through an adhesive
layer obtained by curing the adhesive composition described above.
Advantageous Effects of Invention
[0017] According to the present invention, an adhesive composition capable of forming an
adhesive layer which has excellent sterilization resistance and which can maintain
excellent adhesive strength and appearance, even after a sterilization with hydrogen
peroxide plasma, is provided. According to the present invention, an endoscope device
in which an adhesive layer bonding constituent materials to each other or coating
the constituent materials has excellent sterilization resistance and can maintain
excellent adhesive strength and appearance, even after sterilization with hydrogen
peroxide plasma, is provided.
Brief Description of Drawings
[0018]
FIG. 1 is a perspective view showing a schematic configuration of an endoscope according
to one embodiment.
FIG. 2 is a partial cross-sectional side view of a distal tip part of the endoscope
to which outer sheath tube is fixed.
FIG. 3 is a front view of a distal tip part of the endoscope.
Description of Embodiments
[0019] Adhesive compositions according to the embodiments of the present invention and endoscope
devices using the same will be explained below. The adhesive composition of the present
embodiment comprises an ion exchanger in addition to a main agent, a curing agent,
and a filler, and is preferably used as an adhesive for a medical device.
[0020] The main agent contains an acrylic rubber and an epoxy resin. The acrylic rubber
provides moisture resistance and heat resistance capable of standing a sterilization
treatment, in particular a sterilization treatment in high temperature and high pressure
steam, to the adhesive composition, and plays a role to maintain a good the adhesive
strength.
[0021] The acrylic rubber is preferably used in a state of a fine powder having an average
particle size of 300 nm or less. The acrylic rubber can be used in a state in which
the rubber is dispersed in an epoxy resin described below (a bisphenol A epoxy resin,
a bisphenol F epoxy resin, or a phenol novolac epoxy resin). When the epoxy resin
in which the acrylic rubber is dispersed is heated, a sea-island structure in which
the acrylic rubber is distributed like islands in the epoxy resin is formed. As a
result, it is easy to exhibit the adhesive properties such as the sterilization resistance
even in high temperature and high humidity conditions.
[0022] It is generally said that the formation of the sea-island structure has a tendency
to depend on the mixing condition or the curing condition of the epoxy resin and the
acrylic rubber; however, when the acrylic rubber is dispersed in the epoxy resin,
the sea-island structure can be easily formed without depending too much on the mixing
condition or curing condition, whereby flexibility in the bonding work or the curing
condition can be increased.
[0023] The content of the acrylic rubber is preferably from about 1 to 20% by mass of the
total amount of the main agent. When the acrylic rubber is contained, the crosslinking
density can be increased in addition to the adhesion shear strength and the adhesion
peel strength, thus resulting in improved autoclave resistance or chemical resistance
of the cured product. As a result, even if the sterilization treatment in high temperature
and high pressure steam or the sterilization treatment using the chemical is performed,
an adhesive composition capable of exhibiting sufficient adhesive strength can be
easily obtained. The content of the acrylic rubber is more preferably from about 5
to 15% by mass of the total amount of the main agent. Specifically, AC-3365 (manufactured
by Aika Kogyo Co., Ltd.) and the like can be used as the acrylic rubber.
[0024] The epoxy resin in the main agent contains at least one resin selected from bisphenol
A epoxy resins, bisphenol F epoxy resins, and phenol novolac epoxy resins.
[0025] It is preferable to contain three kinds of epoxy resin, bisphenol A epoxy resin,
bisphenol F epoxy resin, and phenol novolac epoxy resin, because the adhesive layer
having high sterilization resistance, appropriate viscosity, and high adhesive strength
can be obtained, even if the sterilization treatment is repetitively performed.
[0026] The content of the bisphenol A epoxy resin is preferably from about 20 to 70 parts
by weight, based on 100 parts by mass of the main agent, more preferably from 30 to
60 parts by weight. Specifically, JER 828 (manufactured by Mitsubishi Chemical Corporation)
and the like can be used as the bisphenol A epoxy resin.
[0027] The content of the bisphenol F epoxy resin is preferably from about 10 to 60 parts
by mass, based on 100 parts by mass of the main agent, more preferably about from
30 to 60 parts by mass. Specifically, JER 807 (manufactured by Mitsubishi Chemical
Corporation) and the like can be used as the bisphenol F epoxy resin.
[0028] The content of the phenol novolac epoxy resin is preferably from about 20 to 40 parts
by weight, based on 100 parts by mass of the main agent, more preferably from about
30 parts by weight. Specifically, N-770 (manufactured by DIC Corporation) and the
like can be used as the phenol novolac epoxy resin.
[0029] Xylylene diamine can be used as the curing agent, and the curing agent may further
contain a derivative thereof. The xylylene diamine and the derivative thereof may
be called as an "amine-based curing agent." When the derivative thereof is contained
together with the xylylene diamine, the reaction speed with the main agent can be
increased. The examples of the derivative of the xylylene diamine include alkylene
oxide adducts, glycidyl ester adducts, glycidyl ether adducts, Mannich adducts, acrylonitrile
adducts, epichlorohydrin adducts, xylylene diamine trimer, and the like.
[0030] Meta-Xylylene diamine is preferable, because it has an aromatic backbone and is structurally
rigid.
[0031] When the xylylene diamine derivative is used, the content thereof is preferably from
about 10 to 99% by mass of the total amount of the curing agent, more preferably from
about 30 to 97% by mass. When the xylylene diamine and the derivative thereof is contained
in the range described above, the appropriate reaction speed can be obtained, and
effects of suppression of a reaction with carbonic acid gas in the air and improvement
of the adhesive strength can also be obtained.
[0032] In addition to the amine-based curing agent as described above, another compound
may be contained as the curing agent. The examples of other compound include polyamide
resins, imidazoles, acid anhydrides, and the like.
[0033] It is desired that the blending ratio of the main agent and the curing agent is adjusted
so that the epoxy groups in the epoxy resin in the main agent are equivalent to the
functional groups reacting with the epoxy groups in the curing agent.
[0034] Regarding the epoxy resin, a molecular weight per function is referred to as an epoxy
equivalent, and an amine equivalent of the amine-based curing agent is referred to
as an active hydrogen equivalent. A theoretical blending ratio is calculated from
the epoxy equivalent and the amine equivalent, and an optimum blending ratio is determined
from the adhesive strength, and the like, using the theoretical blending ratio as
a guide to an appropriate blending ratio.
[0035] The blending ratio (mass ratio) of the main agent to the curing agent is preferably
from 10 : 1 to 10 : 9. When the main agent and the curing agent are contained in this
pre-determined blending ratio, disadvantages such as oxidative deterioration, softening
deterioration caused by hydrolysis or heat, curing deterioration, brittle fracture
and reduction of the adhesive strength can be avoided. The blending ratio of the main
agent to the curing agent is more preferably from 10 : 1 to 10 : 7.
[0036] The adhesive composition of the present embodiment contains silica as the filler.
Silica may be, for example, spherical silica having an average particle size of 4
µm or more and 7 µm or less. The content thereof is preferably from 20 to 40 parts
by mass based on 100 parts by mass of the adhesive main agent. Here, the average particle
size is a volume-based average particle size, and can be obtained in a usual manner.
[0037] The shape of the silica can be determined by observation with an electronic microscope.
The silica which can be used includes fused silica such as spherical silica produced
by fusing natural quartz crystals with a burner. More specifically, HPS-3500 (manufactured
by Toagosei Co., Ltd.) and the like can be used.
[0038] The adhesive composition of the present embodiment contains an ion exchanger in addition
to the main agent, the curing agent and the filler.
[0039] The deterioration of the adhesive layer during the hydrogen peroxide plasma sterilization
is caused by the sterilizing gas attacking the adhesive layer, which cuts polymerization
parts in the resin forming the adhesive layer. Thus if the sterilizing gas can be
trapped, the disadvantage described above can be avoided, and the sterilization resistance
can be improved. The present inventors have found that the ion exchanger effectively
acts as a material trapping the sterilizing gas.
[0040] The ion exchanger is a substance having an ion exchange capability, and it is preferably
contained in an amount of 0.8 to 12 parts by mass based on 100 parts by mass of the
main agent. When the ion exchanger is contained in an amount of 1 to 5 parts by mass
based on 100 parts by mass of the main agent, the adhesive layer having more excellent
properties can be formed.
[0041] The examples of the ion exchanger include organic ion exchangers containing at least
one compound selected from the group consisting of styrene, divinyl benzene, and derivatives
thereof. The examples of the organic ion exchanger which can be used, include Amberlite
(manufactured by Organodaw Chemical Company), and DIAION AMP 03 (manufactured by Mitsubishi
Chemical Corporation), and the like.
[0042] As the ion exchanger, an inorganic ion exchanger may be used which contains at least
one member selected from bismuth, antimony, zirconium, magnesium, and aluminum as
a main component. Specifically, the examples of the inorganic ion exchanger which
can be used, include IXE-500 (manufactured by TOAGOSEI Co., Ltd.), and the like.
[0043] The adhesive composition of the present embodiment can form the adhesive layer, which
has the excellent sterilization resistance and which can maintain excellent adhesive
strength and appearance, even if the sterilization treatment using the hydrogen peroxide
plasma is performed, because the composition contains the ion exchanger. Moreover,
the adhesive composition of the present embodiment has a viscosity appropriate for
forming an adhesive layer having no defects, and has a good workability.
[0044] The adhesive composition of the present embodiment may contain fumed silica in a
content of about 0.1 to 5% of the total mass of the adhesive, in order to increase
thixotropy considering the workability.
[0045] The adhesive composition of the present embodiment may further contain additives
such as a catalyst, an adhesiveness imparting agent, a solvent, a plasticizer, an
antioxidant, a polymerization inhibitor, a surfactant, an antifungal agent, and a
coloring agent. These additives may be previously added to the main agent, or may
be added to a mixture of the main agent and the curing agent.
[0046] Using the adhesive composition described above, parts of an endoscope can be bonded
to each other, for example, in a method described below.
[0047] First, a liquid containing the main agent and a liquid containing the curing agent
are mixed in a pre-determined ratio, to which the filler and the ion exchanger are
added. Then, the obtained mixture is coated on surfaces of given endoscope parts to
be applied using a brush or the like, and the parts are bonded and fixed. After that,
the assembly is heated at a pre-determined temperature for a pre-determined time,
thereby strongly bonding the endoscope parts to each other.
[0048] Sealing of an imaging device of the endoscope, and exterior finishing and fixing
of edges of the flexible sheath tube can be performed in the same manner as above.
Furthermore, the adhesive layer can be built up around lenses for observation or lenses
for illumination in the same manner as above.
[0049] The heating temperature varies depending on the kind and the blending ratio of the
main agent and the curing agent contained in the adhesive composition, and is preferably
about 60 to 135°C. When the heating temperature is within the range described above,
the curing reaction can proceed at a practical speed. Moreover, endoscope parts having
a low heat resistance are not thermally deteriorated. The heating time is preferably
from about 0.5 to 3 hours.
[0050] The members bonded using the adhesive composition described above are not particularly
limited so long as they are members constituting the endoscope device. For example,
using the adhesive composition of the present embodiment, open parts of various tubes,
which are incorporated into an insertion part of an endoscope device, can be fixed
on a tip part of the insertion part or an operation part. It is also possible to fix
lenses, disposed on a hard part in the tip part of the insertion part, on a lens frame
or the hard part in the tip part. It is further possible to fix a fiber bundle, which
is incorporated in the insertion part, on the lens frame or the hard part in the tip
part. The adhesive composition of the present embodiment can also be used for protecting
and fixing CCD, which is incorporated in the hard part in the tip part.
[0051] When the exterior finishing is performed using the adhesive composition of the present
embodiment, the insertion property can be secured. Specifically, the edge of a flexible
sheath tube in the insertion part of the endoscope device is tightly bound with threads
from the outside, thus, the edge of a flexible sheath tube is fixed on a member inside
thereof. The securing of the insertion property by the exterior finishing and the
preventing threads from fraying can be attained at the same time by coating the tightly
bounded thread with the adhesive composition.
[0052] Referring to the drawings, the endoscope device using the adhesive composition of
the present embodiment will be explained below.
[0053] As shown in FIG. 1, the endoscope device 1 of the present embodiment comprises a
thin and long insertion part 2, which is to be inserted into a body of a subject;
an operation part 7, which is connected to the insertion part 2; and a universal cord
8, which is electrically connected to the operation part 7 and supplies illumination
light.
[0054] A tip part 3 at a tip of the insertion part 2 irradiates illumination light from
the tip, and receives reflection light from the inside of the body. A bendable part
4 and a flexible tube 5 contain optical fibers transmitting light received at the
tip part 3, and can be bent.
[0055] In such an endoscope device 1, members to be bonded using the adhesive composition
are not particularly limited so long as they are members constituting the endoscope
device 1. A use mode in the present embodiment is explained below by examples.
[0056] In the tip part 3 of the endoscope device 1, as shown in FIG. 2, a light guide fiber
21, which supplies illumination light, and a hard part 23 in the tip part, which holds
an imaging unit 22 and is in the shape of a cylindrical block are provided, and a
tip part cover 24 is fitted around a side surface of the hard part 23 in the tip part.
An adhesive layer 25 using the adhesive composition described above is provided at
a section where the hard part 23 in the tip part and the tip part cover 24 are fitted,
and bonds them.
[0057] A tubular bendable rubber 31, which covers a periphery of the bendable part 4, is
externally fitted at the base end side of the tip part cover 24. Threads are wound
around the bendable rubber 31 and tightly bound at the externally fitted part of the
bendable rubber 31 to form a thread wound part 34, whereby the bendable rubber 31
is fixed on the tip part cover 24. An adhesive layer 36 using the adhesive composition
described above is formed on a periphery of the thread wound part 34, whereby the
securing of the insertion property by the exterior finishing and the preventing threads
from fraying can be attained at the same time. The adhesive layer 36 covers the thread
wound part 34 along the side surfaces of the tip part cover 24 and the bendable rubber
31. When the insertion part 2 is inserted, the tip part 3 and the bendable part 4
come into contact with a living body and can slide smoothly.
[0058] In the endoscope device 1, using the adhesive composition described above, open parts
of various tubes, which are incorporated into the insertion part 2 of the endoscope
device 1, can be fixed on the tip part of the insertion part 2 and the operation part
7. Lenses 22a, disposed on the hard part 23 in the tip part of the insertion part
2, may be fixed on a lens frame or the hard part 23 in the tip part. A fiber bundle,
which is incorporated in the insertion part 2, may also be fixed on a lens frame or
the hard part 23 in the tip part. Further, CCD of the imaging unit 22, put in the
tip part 3, can be provided, fixed and sealed.
[0059] A periphery of a connection part of the bendable part 4 and the flexible tube 5,
which are not shown in drawings, has the same structure as that of the periphery of
the connection part of the tip part 3 and the bendable part 4. Specifically, at the
connection part of the bendable part 4 and the flexible tube 5, a thread wound part
is formed, and a periphery of the thread wound part is coated with the same adhesive
composition as above. when the adhesive layer using such an adhesive composition is
provided, the securing of the insertion property by the exterior finishing and the
preventing threads from fraying can be attained at the same time.
[0060] Imaging elements of the endoscope device can also be sealed using the adhesive composition
described above. It is also possible to build up the adhesive composition around lenses
for observation or lenses for illumination in the endoscope device to smooth corners
of the lens peripheries.
[0061] The adhesive composition of the present embodiment may also be disposed around the
lens frame in the tip part 3 of the endoscope device 1.
[0062] FIG. 3 is a front view of the tip part 3 of the endoscope 1. A forceps channel 42
is provided in an insulating member 41. An objective lens 45 is disposed between two
illumination lenses 46, and an adhesive 49 is filled in a space between the illumination
lens 46 and a frame 43 for the objective lens to form a partition 48. This structure
prevents direct incidence of light from the illumination lens 46 to the objective
lens 45, and fixes the illumination lenses 46 and the frame 43 for the objective lens
with the adhesive layer 49.
[0063] As described above, in the present embodiment, the ion exchanger is blended with
the adhesive composition comprising the main agent containing the acrylic rubber and
the epoxy resin, the curing agent containing the xylylene diamine and the derivative
thereof, and the filler. The epoxy resin is at least one resin selected from the bisphenol
A epoxy resins, bisphenol F epoxy resins, and phenol novolac epoxy resin.
[0064] When such an adhesive composition is used, it is possible to form the adhesive layer
which has the excellent sterilization resistance and which can maintain excellent
adhesive strength and appearance, even after a sterilization with the hydrogen peroxide
plasma.
[0065] Moreover, the adhesive composition of the present embodiment has a viscosity appropriate
for bonding members of the endoscope or for work such as exterior finishing. The adhesive
composition described above is used for various applications. For example, it is used
for bonding parts of the endoscope, exterior finishing of the flexible sheath tube
edge in the insertion part of the endoscope and fixing the threads, sealing the imaging
elements of the endoscope, or smoothing the corners of the lens periphery by building
up the adhesive around lenses for observation or lenses for illumination in the endoscope.
It is possible, accordingly, to obtain an endoscope device having an adhesive layer
whose sterilization resistance is not deteriorated so much by any disinfection method.
Example
[0066] Examples of the present invention will be explained below; however, the present invention
is not limited to Examples below.
(Example 1)
[0067] A bisphenol A epoxy resin, a phenol novolac epoxy resin, and an acrylic rubber were
mixed to prepare a main agent. Amounts (parts by mass) of the components in the main
agent are as follows:
Bisphenol A epoxy resin: 70 parts by mass
Phenol novolac epoxy resin: 30 parts by mass
Acrylic rubber particles: 10 parts by mass
[0068] The main agent prepared as above and meta-xylylene diamine, which was a curing agent,
were mixed in a mass ratio of 10 : 4, and silica, which was a filler, was added to
the obtained mixture. The silica used was spherical fused silica having an average
particle size of 6 µm, and the content thereof was 21% by mass of the total amount
of the composition.
[0069] As an ion exchanger, an organic ion exchanger (Amberlite manufactured by Organodaw
Chemical Company) was prepared, and it was added in an amount of 0.8 parts by mass
based on 100 parts by mass of the main agent, thereby producing an adhesive composition
of Example 1.
[0070] Adhesive compositions of Examples 2 to 18 were obtained in the same manner as in
Example 1, except that the content of the organic ion exchanger was changed to that
shown in Tables 1 and 2 below. Numbers of each component in Tables 1 and 2 express
parts by mass of each component.
[Table 1]
|
Example |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
Main agent |
Bisphenol A epoxy resin (JER 828, Mitsubishi Chemical Corporation) |
70 |
70 |
70 |
70 |
70 |
70 |
- |
- |
- |
Bisphenol F epoxy resin (JER 807, Mitsubishi Chemical Corporation) |
- |
- |
- |
- |
- |
- |
70 |
70 |
70 |
Acryric rubber (AC-3365, Aika Kogyo Co., Ltd.) |
10 |
10 |
10 |
10 |
10 |
10 |
10 |
10 |
10 |
Phenol novolac epoxy resin (N-770, DIC Corporation) |
30 |
30 |
30 |
30 |
30 |
30 |
30 |
30 |
30 |
Curing agent |
meta-xylylene diamine (Mitsubishi Gas Chemical Company, Ind.) |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
Filler |
Silica (HPS-3500, Toagosei Co., Ltd.) |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
Ion exchanger (Amberlite, Organodaw Chemical Company) |
0.8 |
1 |
3 |
5 |
10 |
12 |
0.8 |
1 |
3 |
[Table 2]
|
Example |
10 |
11 |
12 |
13 |
14 |
15 |
16 |
17 |
18 |
Main agent |
Bisphenol A epoxy resin (JER 828, Mitsubishi Chemical Corporation) |
- |
- |
- |
10 |
10 |
10 |
10 |
10 |
10 |
Bisphenol F epoxy resin (JER 807, Mitsubishi Chemical Corporation) |
70 |
70 |
70 |
35 |
35 |
35 |
35 |
35 |
35 |
Acryric rubber (AC-3365, Aika Kogyo Co., Ltd.) |
10 |
10 |
10 |
35 |
35 |
35 |
35 |
35 |
35 |
Phenol novolac epoxy resin (N-770, DIC Corporation) |
30 |
30 |
30 |
30 |
30 |
30 |
30 |
30 |
30 |
Curing agent |
meta-xylylene diamine (Mitsubishi Gas Chemical Company, Ind.) |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
Filler |
Silica (HPS-3500, Toagosei Co., Ltd.) |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
40 |
Ion exchanger (Amberlite, Organodaw Chemical Company) |
5 |
10 |
12 |
0.8 |
1 |
3 |
5 |
10 |
12 |
[0071] Adhesive compositions of Comparative Examples 1 to 3 were obtained in the same manner
as in Example 1, except that the composition was changed to that shown in Table 3
below. Numbers in each component in Table 3 express parts by mass of each component.
[Table 3]
|
Comparative Example |
1 |
2 |
3 |
Main agent |
Bisphenol A epoxy resin (JER 828, Mitsubishi Chemical Corporation) |
70 |
- |
10 |
Bisphenol F epoxy resin (JER 807, Mitsubishi Chemical Corporation) |
- |
70 |
35 |
Acryric rubber (AC-3365, Aika Kogyo Co., Ltd.) |
10 |
10 |
35 |
Phenol novolac epoxy resin (N-770, DIC Corporation) |
30 |
30 |
30 |
Curing agent |
meta-xylylene diamine (Mitsubishi Gas Chemical Company, Ind.) |
40 |
40 |
40 |
Filler |
Silica (HPS-3500, Toagosei Co., Ltd.) |
40 |
40 |
40 |
Ion exchanger (Amberlite, Organodaw Chemical Company) |
- |
- |
- |
[0072] A viscosity of each of the adhesive compositions of Examples 1 to 18 and Comparative
Examples 1 to 3 was determined at 25°C and the workability was evaluated based on
the viscosity in accordance with the criteria described below. The smaller the viscosity,
the better the workability, but the workability is good with no problem when the viscosity
is 200 Pa·s or lower.
- A: Lower than 100 Pa·s
- B: 100 Pa·s or higher and 200 Pa·s or lower
[0073] An adhesive layer was formed from each resin composition by heating stainless steel
test pieces at 80°C for 2 hours to cure the resin composition. A tensile shearing
strength was determined using the test pieces bonded to obtain an SUS-SUS adhesive
strength at the initial stage. The tensile shearing strength was measured in accordance
with JIS K 6850 [Test method for tensile shearing adhesive strength of adhesives].
[0074] The stainless steel test pieces bonded were put in a low temperature plasma sterilization
apparatus, and a sterilization treatment was performed using hydrogen peroxide plasma.
After that, the test described above was performed to obtain an SUS-SUS adhesive strength
after the gas sterilization. When the adhesive strength was 10 MPa or more even after
the gas sterilization treatment, it was considered a pass grade (good). When the adhesive
strength was less than 10 MPa after the gas sterilization treatment, it was considered
inferior.
[0075] The appearance of the adhesive layer was visually observed after the gas sterilization,
and evaluation was made in accordance with the criteria described below:
- A: No change in the appearance (excellent)
- B: No bubbles or cracks were generated, but gloss was reduced on the surface (good)
- C: A number of bubbles or cracks were generated (inferior)
[0076] The obtained results of the workability and the adhesive strengths before and after
the sterilization are summarized in Tables 4, 5 and 6 together with an overall evaluation.
The overall evaluation was performed in accordance with the criteria described below
according to the workability, the adhesive strengths before and after gas sterilization,
and the appearance.
- A: All items were excellent.
- B: The workability or the appearance after the sterilization was "B".
- C: Both of the adhesive strength and the appearance were inferior.
[Table 4]
|
Example |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
Workability |
A |
A |
A |
A |
B |
B |
A |
A |
A |
SUS-SUS adhesive strength (MPa) |
at initial stage |
20 |
21 |
19 |
19 |
18 |
17 |
20 |
20 |
20 |
after gas sterilization |
10 |
15 |
16 |
16 |
12 |
13 |
10 |
15 |
16 |
Appearance after gas sterilization |
B |
A |
A |
A |
A |
A |
B |
A |
A |
Overall evaluation |
B |
A |
A |
A |
B |
B |
B |
A |
A |
[Table 5]
|
Example |
10 |
11 |
12 |
13 |
14 |
15 |
16 |
17 |
18 |
Workability |
A |
B |
B |
A |
A |
A |
A |
B |
B |
SUS-SUS adhesive strength (MPa) |
at initial stage |
19 |
18 |
17 |
20 |
20 |
22 |
19 |
18 |
17 |
after gas sterilization |
16 |
12 |
13 |
10 |
15 |
16 |
16 |
12 |
13 |
Appearance after gas sterilization |
A |
A |
A |
B |
A |
A |
A |
A |
A |
Overall evaluation |
A |
B |
B |
B |
A |
A |
A |
B |
B |
[Table 6]
|
Comparative Example |
1 |
2 |
3 |
Workability |
A |
A |
A |
SUS-SUS adhesive strength (MPa) |
at initial stage |
19 |
18 |
21 |
after gas sterilization |
4 |
3 |
5 |
Appearance after gas sterilization |
C |
C |
C |
Overall evaluation |
C |
C |
C |
[0077] As shown in Tables 4 and 5 above, when the adhesive composition containing the ion
exchanger was used (Examples 1 to 18), the adhesive strength reached the pass level
for all compositions after the gas sterilization. Moreover, all of the adhesive compositions
of Examples had the excellent workability. In particular, it is known that in the
case of the adhesive compositions containing the ion exchanger in the range of 1 to
5 parts by mass based on 100 parts by mass of the main agent (Examples 2 to 4, 8 to
10, and 14 to 16), the adhesive layer having a particularly excellent overall evaluation
can be obtained, and workability of the adhesive composition is extremely excellent.
[0078] On the contrary, in the case of containing no ion exchanger (Comparative Examples
1 to 3), as shown in Table 6 above, the adhesive strength after the gas sterilization
is remarkably low, such as 3 to 5 MPa. This is caused because gas cannot be trapped
during the gas sterilization because of the absence of the ion exchanger, the thus
the adhesive layer is damaged by the sterilizing gas.
[0079] The adhesive composition containing no ion exchanger cannot form the adhesive layer
which has the excellent sterilization resistance and which maintains excellent adhesive
strength or appearance after the hydrogen peroxide plasma sterilization; that is,
it was confirmed that if the ion exchanger is not contained, the object of the present
invention cannot be attained.
[0080] Each of the adhesive compositions of Examples 1 to 18 and Comparative Examples 1
to 3 were coated on parts of an endoscope device, and a curing reaction was performed
at 80°C for 2 hours in the state in which the parts were bonded to each other.
[0081] An edge of a flexible sheath tube, which was a part of the endoscope, in an insertion
part, was tightly bound with threads from the outside and was fixed on a member inside
thereof. Then, the tread was coated with the adhesive composition described above,
thereby carrying out exterior finishing. An imaging device of the endoscope device
was sealed using the adhesive composition.
[0082] An adhesive layer was formed by building up the adhesive composition around lenses
for observation or lenses for illumination of the endoscope device, whereby the corners
of the peripheries of the observation lens and the illumination lens were smoothed.
As described above, the assembly operation of the endoscope device could be performed
with no problem.
[0083] The obtained endoscope device was subjected to the same sterilization treatment using
hydrogen peroxide plasma as above, and the adhesive strength and the appearance of
the adhesive layer after the sterilization treatment were determined. As a result,
no change in the appearance of the adhesive layer was observed after the gas sterilization,
and the adhesive strength was excellent.
[0084] The present invention is not limited to the Examples above, and it can be carried
out in various modifications without departing from the scope of the invention.
[0085] According to the explanation described above, an example in which the endoscope device
is used as a medical device to which the adhesive composition is applied is used,
but the medical device is not particularly limited so long as it is a device which
is used by bringing it into contact with a living body or inserting it into the body.
The medical device may include, for example, an endoscope device, various devices
for surgery, a cell extracting device, a blood component separation device, a blood
transfusion device, and the like.
Reference Signs List
[0086] 1 ... endoscope device; 2 ... insertion part; 3 ... tip part; 4 ...bendable part;
5 ... flexible tube; 7 ... operation part; 8 ... universal cord; 21 ... light guide
fiber; 22 ... imaging unit; 22a ... lenses; 23 ... hard part in tip part; 24 ... tip
part cover; 25 ... adhesive layer; 31 ... curved rubber; 34 ... thread wound part;
36 ... adhesive layer; 41 ... insulating member; 42 ... forceps channel; 43 ... frame
for objective lens; 45 ... objective lens; 46 ... illumination lens; 48 ... partition;
49 ... adhesive layer